Rinu Susan Thomas

English Faculty at Scm Hub International Logistics Business School
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Contact Information
us****@****om
(386) 825-5501
Location
Ernakulam, Kerala, India, IN

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Credentials

  • NSQF- LEVEL 6 A Grade Certified Communicative English Trainer/ Soft Skills Trainer
    National Skill Development Corporation
    Jun, 2022
    - Nov, 2024
  • APTIS- C Grade
    British Council
    Mar, 2022
    - Nov, 2024

Experience

    • India
    • Education Administration Programs
    • 1 - 100 Employee
    • English Faculty
      • Sep 2022 - Present

    • India
    • E-learning
    • 1 - 100 Employee
    • Communicative English / Soft skill Trainer
      • Feb 2022 - Present

    • India
    • Higher Education
    • 1 - 100 Employee
    • OET / Language Trainer
      • Nov 2021 - Jan 2022

      Providing well-structured training to healthcare professionals to impart effective result. Adaptable training methodologies to improve student skill set. Mentored and tutored struggling students individually. Conducted skill evaluation and identified performance gap. Handled interactive classroom sessions. Providing well-structured training to healthcare professionals to impart effective result. Adaptable training methodologies to improve student skill set. Mentored and tutored struggling students individually. Conducted skill evaluation and identified performance gap. Handled interactive classroom sessions.

    • United States
    • Pharmaceutical Manufacturing
    • 700 & Above Employee
    • Clinical Data Associate
      • 2010 - 2011

      • Query management, raising lock requests, manual review and report generation using Medidata Rave. • Generate, review and submit data listings, metrics/reports and quality control documentation to support business needs. • Review and process clinical data to ensure database accuracy and consistency. • Review outstanding discrepancies to query the site to take actions. • Tracking CRF’s, lab data reconciliation, marking off missing pages. • Data management status report generation. • Query management, raising lock requests, manual review and report generation using Medidata Rave. • Generate, review and submit data listings, metrics/reports and quality control documentation to support business needs. • Review and process clinical data to ensure database accuracy and consistency. • Review outstanding discrepancies to query the site to take actions. • Tracking CRF’s, lab data reconciliation, marking off missing pages. • Data management status report generation.

    • United States
    • Higher Education
    • 700 & Above Employee
    • Research Associate
      • Mar 2009 - Nov 2010

      • Requirement gathering, analysis and development of business specification document. • DB modeling (logical/physical schema) and database building using My SQL Workbench • Data analysis of legacy databases, create data mapping and transformation rules for migration. • Performed data profiling for data cleanup in source for better data transformation • Devised data parsers and SQL query development for data retrieval/update/insert. • Requirement gathering, analysis and development of business specification document. • DB modeling (logical/physical schema) and database building using My SQL Workbench • Data analysis of legacy databases, create data mapping and transformation rules for migration. • Performed data profiling for data cleanup in source for better data transformation • Devised data parsers and SQL query development for data retrieval/update/insert.

    • United States
    • IT Services and IT Consulting
    • 700 & Above Employee
    • Programmer Analyst
      • Sep 2007 - Jun 2008

      • Design and Development of Electronic Case Report Forms(CRF) according to Protocol using CDMS tool CLINTRIAL and INFORM • Creation and modification of CLINTRIAL objects for ORACLE databases. • Building up study set-up and Analyzing Edit Check specifications • Testing of Study to verify if the same meets the specified requirements • Understanding on Pharmaceutical research and drug discovery process including different phases of clinical trials. • Design and Development of Electronic Case Report Forms(CRF) according to Protocol using CDMS tool CLINTRIAL and INFORM • Creation and modification of CLINTRIAL objects for ORACLE databases. • Building up study set-up and Analyzing Edit Check specifications • Testing of Study to verify if the same meets the specified requirements • Understanding on Pharmaceutical research and drug discovery process including different phases of clinical trials.

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